Canonical Allele Identifier: CA228625588

Gene: DRD2

Linked Data

• dbSNP Id: rs202098964
• gnomAD v2: 11-113283346-G-A
• gnomAD v3: 11-113412624-G-A
• gnomAD v4: 11-113412624-G-A
• MyVariant Identifiers: chr11:g.113283346G>A (hg19) ; chr11:g.113412624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412624G>A , CM000673.2:g.113412624G>A	GRCh38
NC_000011.9:g.113283346G>A , CM000673.1:g.113283346G>A	GRCh37
NC_000011.8:g.112788556G>A	NCBI36
NG_008841.1:g.67656C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1070C>T MANE Select	ENSP00000354859.3:p.Thr357Ile
ENST00000346454.7:c.983C>T	ENSP00000278597.5:p.Thr328Ile
ENST00000362072.7:c.1070C>T	ENSP00000354859.3:p.Thr357Ile
ENST00000538967.5:c.1076C>T	ENSP00000438215.1:p.Thr359Ile
ENST00000542968.5:c.1070C>T	ENSP00000442172.1:p.Thr357Ile
ENST00000544518.5:c.1067C>T	ENSP00000441068.1:p.Thr356Ile
NM_000795.3:c.1070C>T	NP_000786.1:p.Thr357Ile
NM_016574.3:c.983C>T	NP_057658.2:p.Thr328Ile
XM_017017296.2:c.1070C>T	XP_016872785.1:p.Thr357Ile
NM_000795.4:c.1070C>T MANE Select	NP_000786.1:p.Thr357Ile
NM_016574.4:c.983C>T	NP_057658.2:p.Thr328Ile